Item | Value |
---|---|
geneid | 139716 |
ensemblid | ENSG00000160219.12 |
hgncid | 17515 |
symbol | GAB3 |
name | GRB2 associated binding protein 3 |
refseq_nuc | NM_001081573.3 |
refseq_prot | NP_001075042.1 |
ensembl_nuc | ENST00000424127.3 |
ensembl_prot | ENSP00000399588.2 |
mane_status | MANE Select |
chr | chrX |
start | 154675249 |
end | 154751077 |
strand | - |
ver | v1.2 |
region | chrX:154675249-154751077 |
region5000 | chrX:154670249-154756077 |
regionname0 | GAB3_chrX_154675249_154751077 |
regionname5000 | GAB3_chrX_154670249_154756077 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 587 | 241 | 71 | 50 | 88 | 10 | 20 | 74 | GAB3_chrX_154670249_154756077 | GAB3 | MSAGD others(582): Show |
chrX | 154670249 | 154756077 |
a0002 | 0/0 | 587 | 6 | 0 | 0 | 5 | 0 | 1 | 5 | GAB3_chrX_154670249_154756077 | GAB3 | MSAGD others(582): Show |
chrX | 154670249 | 154756077 |
a0003 | 0/0 | 587 | 4 | 0 | 1 | 0 | 1 | 2 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | MSAGD others(582): Show |
chrX | 154670249 | 154756077 |
a0004 | 0/0 | 587 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | MSAGD others(582): Show |
chrX | 154670249 | 154756077 |
a0005 | 0/0 | 587 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | MSAGD others(582): Show |
chrX | 154670249 | 154756077 |
a0006 | 0/0 | 587 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | MSAGD others(582): Show |
chrX | 154670249 | 154756077 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1761 | 233 | 64 | 50 | 87 | 10 | 20 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 | ||
a0001c0002 | 0/0 | 1761 | 7 | 7 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 | ||
a0001c0006 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 | ||
a0002c0003 | 0/0 | 1761 | 6 | 0 | 0 | 5 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 | ||
a0003c0004 | 0/0 | 1761 | 4 | 0 | 1 | 0 | 1 | 2 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 | ||
a0004c0005 | 0/0 | 1761 | 4 | 3 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 | ||
a0005c0008 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 | ||
a0006c0007 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | ATGAG others(1756): Show |
chrX | 154670249 | 154756077 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4745 | 84 | 3 | 21 | 46 | 4 | 9 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0002 | 1/0 | 4745 | 42 | 26 | 2 | 3 | 1 | 9 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0003 | 0/0 | 4745 | 37 | 1 | 21 | 12 | 1 | 2 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0004 | 0/0 | 4744 | 12 | 11 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4739): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0005 | 0/0 | 4745 | 13 | 0 | 1 | 10 | 2 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0006 | 0/0 | 4745 | 11 | 10 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0007 | 0/0 | 4744 | 8 | 0 | 0 | 8 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4739): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0008 | 0/0 | 4744 | 7 | 7 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4739): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0009 | 0/0 | 4746 | 5 | 0 | 1 | 4 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4741): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0010 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4739): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0011 | 0/0 | 4745 | 2 | 0 | 0 | 0 | 2 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0012 | 0/0 | 4745 | 2 | 0 | 2 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0013 | 0/0 | 4746 | 2 | 0 | 0 | 2 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4741): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0014 | 0/0 | 4745 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0015 | 0/0 | 4745 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0016 | 0/0 | 4745 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0017 | 0/0 | 4745 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0018 | 0/0 | 4745 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0020 | 0/0 | 4745 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0001t0022 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4741): Show |
chrX | 154670249 | 154756077 |
a0001c0002t0002 | 0/0 | 4745 | 4 | 4 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0001c0002t0004 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4739): Show |
chrX | 154670249 | 154756077 |
a0001c0002t0010 | 0/0 | 4744 | 2 | 2 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4739): Show |
chrX | 154670249 | 154756077 |
a0001c0006t0019 | 0/0 | 4745 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0002c0003t0001 | 0/0 | 4745 | 6 | 0 | 0 | 5 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0003c0004t0003 | 0/0 | 4745 | 3 | 0 | 1 | 0 | 1 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0003c0004t0021 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4741): Show |
chrX | 154670249 | 154756077 |
a0004c0005t0002 | 0/0 | 4745 | 4 | 3 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
a0005c0008t0009 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4741): Show |
chrX | 154670249 | 154756077 |
a0006c0007t0001 | 0/0 | 4745 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | CTTCT others(4740): Show |
chrX | 154670249 | 154756077 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0007g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0008g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0009g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0011g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0012g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0012g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0013g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0016g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0018g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0020g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0001t0022g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0002t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0002t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0001c0006t0019g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0003c0004t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0003c0004t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0003c0004t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0003c0004t0021g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0004c0005t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0004c0005t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0004c0005t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0004c0005t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0005c0008t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
a0006c0007t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | GBR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | GBR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0190 | EAS | CHS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01081 | hp2 | a0003 | c0004 | t0003 | g0126 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0197 | AMR | PUR | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0203 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01515 | hp1 | a0001 | c0001 | t0011 | g0006 | EUR | IBS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0204 | EUR | IBS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01517 | hp1 | a0001 | c0001 | t0011 | g0006 | EUR | IBS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0086 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01891 | hp2 | a0004 | c0005 | t0002 | g0053 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01928 | hp1 | a0001 | c0001 | t0012 | g0185 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01934 | hp1 | a0004 | c0005 | t0002 | g0091 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01943 | hp1 | a0001 | c0001 | t0012 | g0132 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02027 | hp1 | a0001 | c0006 | t0019 | g0233 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02148 | hp2 | a0001 | c0001 | t0009 | g0146 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02717 | hp1 | a0001 | c0002 | t0010 | g0052 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0196 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0019 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02965 | hp1 | a0004 | c0005 | t0002 | g0049 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03041 | hp2 | a0001 | c0001 | t0016 | g0042 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03098 | hp1 | a0001 | c0001 | t0017 | g0018 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0084 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03225 | hp1 | a0001 | c0001 | t0018 | g0087 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0116 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03669 | hp2 | a0003 | c0004 | t0021 | g0106 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0155 | SAS | PJL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | BEB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG04115 | hp1 | a0003 | c0004 | t0003 | g0169 | SAS | STU | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | BEB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG04199 | hp1 | a0005 | c0008 | t0009 | g0118 | SAS | STU | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | YRI | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18612 | hp1 | a0006 | c0007 | t0001 | g0024 | EAS | CHB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | YRI | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | YRI | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18941 | hp2 | a0001 | c0001 | t0020 | g0173 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18949 | hp2 | a0001 | c0001 | t0013 | g0021 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18953 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18979 | hp2 | a0001 | c0001 | t0009 | g0097 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0127 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18985 | hp1 | a0001 | c0001 | t0009 | g0186 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18989 | hp1 | a0001 | c0001 | t0013 | g0210 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18993 | hp2 | a0001 | c0001 | t0009 | g0208 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19006 | hp1 | a0001 | c0001 | t0009 | g0156 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0090 | AFR | LWK | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0194 | AFR | LWK | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | LWK | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19055 | hp1 | a0001 | c0001 | t0022 | g0170 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19082 | hp1 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19085 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19089 | hp1 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19090 | hp2 | a0002 | c0003 | t0001 | g0139 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0145 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0207 | EUR | TSI | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA20805 | hp1 | a0003 | c0004 | t0003 | g0109 | EUR | TSI | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | GIH | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02109 | hp2 | a0004 | c0005 | t0002 | g0050 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02559 | hp1 | a0001 | c0001 | t0014 | g0010 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG02559 | hp2 | a0001 | c0002 | t0004 | g0048 | AFR | ACB | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0198 | AFR | MSL | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | USA | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | USA | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA18955 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0193 | AFR | USA | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | USA | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | LWK | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
NA21309 | hp2 | a0001 | c0002 | t0010 | g0051 | AFR | LWK | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0065 | REF | REF | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0027 | REF | REF | GAB3_chrX_154670249_154756077 | GAB3 | chrX | 154670249 | 154756077 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154680220 | C | G | 1 | a0002 | 6 | HG03710.hp1 NA18982.hp1 NA19009.hp1 others(3): Show |
missense_variant | MODERATE | c.1559G>C | p.Ser520Thr | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/10 | 1611/4745 | 1559/1764 | 520/587 | chrX | 154680220 | |||
chrX:154695922 | C | T | 1 | a0004 | 4 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(1): Show |
missense_variant | MODERATE | c.1525G>A | p.Glu509Lys | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/10 | 1577/4745 | 1525/1764 | 509/587 | chrX | 154695922 | |||
chrX:154699497 | G | A | 1 | a0006 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.1142C>T | p.Pro381Leu | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/10 | 1194/4745 | 1142/1764 | 381/587 | chrX | 154699497 | |||
chrX:154712334 | G | A | 1 | a0005 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.964C>T | p.Arg322Cys | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/10 | 1016/4745 | 964/1764 | 322/587 | chrX | 154712334 | |||
chrX:154712586 | G | A | 1 | a0003 | 4 | HG01081.hp2 HG03669.hp2 HG04115.hp1 others(1): Show |
missense_variant | MODERATE | c.712C>T | p.Pro238Ser | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/10 | 764/4745 | 712/1764 | 238/587 | chrX | 154712586 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154695938 | G | A | 1 | a0001c0006 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1509C>T | p.Asp503Asp | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/10 | 1561/4745 | 1509/1764 | 503/587 | chrX | 154695938 | |||
chrX:154712659 | T | C | 2 | a0001c0002 a0004c0005 |
11 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(8): Show |
synonymous_variant | LOW | c.639A>G | p.Ser213Ser | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/10 | 691/4745 | 639/1764 | 213/587 | chrX | 154712659 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154675850 | G | C | 1 | a0001c0001t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 2328 | chrX | 154675850 | ||||||
chrX:154675858 | C | G | 2 | a0001c0001t0005 a0001c0001t0013 |
15 | HG01255.hp1 HG01516.hp2 NA18949.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2320G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 2320 | chrX | 154675858 | ||||||
chrX:154676110 | T | C | 1 | a0001c0001t0011 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2068A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 2068 | chrX | 154676110 | ||||||
chrX:154676120 | A | G | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(6): Show |
61 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2058T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 2058 | chrX | 154676120 | ||||||
chrX:154676196 | T | C | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(6): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1982A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 1982 | chrX | 154676196 | ||||||
chrX:154676232 | A | G | 1 | a0001c0001t0006 | 11 | HG01243.hp1 HG02723.hp2 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1946T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 1946 | chrX | 154676232 | ||||||
chrX:154676325 | G | A | 1 | a0001c0001t0017 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1853C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 1853 | chrX | 154676325 | ||||||
chrX:154676540 | T | G | 1 | a0001c0001t0018 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 1638 | chrX | 154676540 | ||||||
chrX:154677179 | G | A | 1 | a0001c0006t0019 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 999 | chrX | 154677179 | ||||||
chrX:154677238 | T | A | 2 | a0001c0001t0020 a0001c0001t0022 |
2 | NA18941.hp2 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*940A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 940 | chrX | 154677238 | ||||||
chrX:154677243 | A | G | 3 | a0001c0001t0004 a0001c0001t0008 a0001c0002t0004 |
20 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*935T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 935 | chrX | 154677243 | ||||||
chrX:154677639 | C | T | 1 | a0001c0001t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*539G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 539 | chrX | 154677639 | ||||||
chrX:154677735 | C | T | 1 | a0001c0001t0008 | 7 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*443G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 443 | chrX | 154677735 | ||||||
chrX:154677921 | T | C | 1 | a0001c0001t0012 | 2 | HG01928.hp1 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*257A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 257 | chrX | 154677921 | ||||||
chrX:154678100 | C | CA | 5 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0022 others(2): Show |
10 | HG02148.hp2 HG03669.hp2 HG04199.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*77dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 77 | chrX | 154678100 | ||||||
chrX:154678100 | CA | C | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(3): Show |
31 | HG00642.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*77delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 10/10 | 77 | chrX | 154678100 | ||||||
chrX:154751067 | C | T | 1 | a0001c0001t0014 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/10 | 42 | chrX | 154751067 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154678731 | G | C | 1 | a0001c0001t0001g0172 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1648-437C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/9 | chrX | 154678731 | |||||||
chrX:154678736 | A | G | 1 | a0001c0001t0005g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1648-442T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/9 | chrX | 154678736 | |||||||
chrX:154678780 | A | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(104): Show |
112 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1648-486T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/9 | chrX | 154678780 | |||||||
chrX:154678851 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1648-557G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/9 | chrX | 154678851 | |||||||
chrX:154679138 | C | T | 2 | a0001c0001t0002g0009 a0001c0001t0002g0215 |
3 | HG03041.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1648-844G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/9 | chrX | 154679138 | |||||||
chrX:154679472 | G | A | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1647+660C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/9 | chrX | 154679472 | |||||||
chrX:154679862 | A | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0098 |
2 | HG00280.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1647+270T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 9/9 | chrX | 154679862 | |||||||
chrX:154680555 | A | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(104): Show |
112 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1531-307T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154680555 | |||||||
chrX:154680950 | C | A | 4 | a0001c0001t0003g0031 a0001c0001t0003g0037 a0001c0001t0003g0047 others(1): Show |
4 | NA18948.hp1 NA18963.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1531-702G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154680950 | |||||||
chrX:154681333 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0232 |
2 | NA18747.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1531-1085G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154681333 | |||||||
chrX:154681435 | GT | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(97): Show |
105 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1531-1188delA | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154681435 | |||||||
chrX:154681891 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1531-1643G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154681891 | |||||||
chrX:154682195 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1531-1947A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154682195 | |||||||
chrX:154683007 | A | C | 1 | a0001c0001t0003g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1531-2759T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154683007 | |||||||
chrX:154683060 | A | T | 3 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0001c0001t0002g0083 |
3 | HG03453.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1531-2812T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154683060 | |||||||
chrX:154683365 | C | T | 1 | a0001c0001t0006g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1531-3117G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154683365 | |||||||
chrX:154683949 | G | C | 7 | a0001c0001t0002g0007 a0001c0001t0002g0092 a0001c0001t0002g0100 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-3701C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154683949 | |||||||
chrX:154684168 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1531-3920A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154684168 | |||||||
chrX:154684468 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1531-4220C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154684468 | |||||||
chrX:154684513 | G | A | 2 | a0001c0001t0020g0173 a0001c0001t0022g0170 |
2 | NA18941.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1531-4265C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154684513 | |||||||
chrX:154684717 | A | T | 1 | a0001c0002t0004g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1531-4469T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154684717 | |||||||
chrX:154686134 | C | T | 6 | a0001c0001t0003g0108 a0001c0001t0003g0110 a0001c0001t0003g0112 others(3): Show |
6 | HG00639.hp1 HG01952.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1531-5886G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154686134 | |||||||
chrX:154686437 | C | CA | 13 | a0001c0001t0001g0064 a0001c0001t0001g0141 a0001c0001t0001g0150 others(10): Show |
14 | HG00735.hp1 HG01516.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1531-6190dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154686437 | |||||||
chrX:154686631 | T | C | 7 | a0001c0001t0002g0007 a0001c0001t0002g0092 a0001c0001t0002g0100 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-6383A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154686631 | |||||||
chrX:154686980 | G | A | 1 | a0001c0001t0006g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1531-6732C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154686980 | |||||||
chrX:154687019 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1531-6771C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687019 | |||||||
chrX:154687023 | C | T | 1 | a0001c0001t0018g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1531-6775G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687023 | |||||||
chrX:154687061 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1531-6813C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687061 | |||||||
chrX:154687291 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1531-7043G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687291 | |||||||
chrX:154687354 | A | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(104): Show |
112 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1531-7106T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687354 | |||||||
chrX:154687506 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1531-7258G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687506 | |||||||
chrX:154687633 | C | CA | 46 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0107 others(43): Show |
46 | HG00735.hp1 HG00735.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1531-7386dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687633 | |||||||
chrX:154687633 | CA | C | 6 | a0001c0001t0001g0230 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1531-7386delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154687633 | |||||||
chrX:154688246 | T | C | 8 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0077 others(5): Show |
13 | HG00733.hp1 HG01074.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1530+7671A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154688246 | |||||||
chrX:154688404 | C | T | 1 | a0001c0001t0007g0131 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1530+7513G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154688404 | |||||||
chrX:154688748 | T | TAGGAAAG others(2731): Show |
1 | a0001c0001t0003g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1530+7168_1530+716 others(2742): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154688748 | |||||||
chrX:154689114 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0002g0100 a0001c0001t0002g0166 |
3 | HG02258.hp1 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1530+6803G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689114 | |||||||
chrX:154689261 | G | T | 193 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(190): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1530+6656C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689261 | |||||||
chrX:154689522 | G | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1530+6395C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689522 | |||||||
chrX:154689711 | G | T | 10 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(7): Show |
10 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1530+6206C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689711 | |||||||
chrX:154689712 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1530+6205T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689712 | |||||||
chrX:154689817 | A | G | 1 | a0001c0001t0017g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1530+6100T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689817 | |||||||
chrX:154689882 | C | A | 21 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(18): Show |
24 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1530+6035G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689882 | |||||||
chrX:154689888 | C | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(99): Show |
107 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1530+6029G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689888 | |||||||
chrX:154689998 | A | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(104): Show |
112 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1530+5919T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689998 | |||||||
chrX:154689999 | C | G | 3 | a0001c0001t0002g0092 a0001c0001t0002g0100 a0001c0001t0002g0166 |
3 | HG02258.hp1 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1530+5918G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154689999 | |||||||
chrX:154690417 | C | G | 3 | a0001c0001t0008g0002 a0001c0001t0008g0086 a0001c0001t0008g0090 |
6 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530+5500G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154690417 | |||||||
chrX:154690418 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1530+5499C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154690418 | |||||||
chrX:154690489 | A | C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0215 |
3 | HG03041.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1530+5428T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154690489 | |||||||
chrX:154690903 | T | C | 21 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(18): Show |
24 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1530+5014A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154690903 | |||||||
chrX:154690904 | G | C | 21 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(18): Show |
24 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1530+5013C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154690904 | |||||||
chrX:154690986 | T | C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0215 |
3 | HG03041.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1530+4931A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154690986 | |||||||
chrX:154691074 | A | G | 1 | a0001c0001t0016g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1530+4843T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154691074 | |||||||
chrX:154691428 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1530+4489A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154691428 | |||||||
chrX:154691479 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1530+4438C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154691479 | |||||||
chrX:154691676 | C | T | 1 | a0001c0001t0004g0222 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1530+4241G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154691676 | |||||||
chrX:154691849 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1530+4068G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154691849 | |||||||
chrX:154691983 | C | A | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1530+3934G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154691983 | |||||||
chrX:154692171 | CA | C | 3 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0001c0001t0002g0083 |
3 | HG03453.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1530+3745delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154692171 | |||||||
chrX:154692175 | A | G | 3 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0001c0001t0002g0083 |
3 | HG03453.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1530+3742T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154692175 | |||||||
chrX:154692220 | A | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0104 |
2 | NA18943.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1530+3697T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154692220 | |||||||
chrX:154692415 | G | T | 4 | a0004c0005t0002g0049 a0004c0005t0002g0050 a0004c0005t0002g0053 others(1): Show |
4 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1530+3502C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154692415 | |||||||
chrX:154692525 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | HG02004.hp1 HG02083.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+3392G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154692525 | |||||||
chrX:154692733 | AGCCGAGC others(23): Show |
A | 1 | a0001c0001t0002g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1530+3154_1530+318 others(34): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154692733 | |||||||
chrX:154692821 | G | C | 1 | a0001c0001t0016g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1530+3096C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154692821 | |||||||
chrX:154693037 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1530+2880A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693037 | |||||||
chrX:154693148 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG03927.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1530+2769T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693148 | |||||||
chrX:154693287 | C | G | 6 | a0001c0001t0003g0108 a0001c0001t0003g0110 a0001c0001t0003g0112 others(3): Show |
6 | HG00639.hp1 HG01952.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530+2630G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693287 | |||||||
chrX:154693505 | G | A | 1 | a0001c0001t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1530+2412C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693505 | |||||||
chrX:154693666 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0134 a0001c0001t0002g0135 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+2251G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693666 | |||||||
chrX:154693667 | G | A | 2 | a0001c0001t0003g0056 a0001c0001t0003g0099 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1530+2250C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693667 | |||||||
chrX:154693861 | G | A | 2 | a0001c0001t0010g0084 a0001c0002t0010g0051 |
2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1530+2056C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693861 | |||||||
chrX:154693978 | C | T | 1 | a0001c0001t0005g0214 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1530+1939G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154693978 | |||||||
chrX:154694035 | G | GA | 8 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(5): Show |
8 | HG02004.hp1 HG02027.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1530+1881dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694035 | |||||||
chrX:154694229 | C | G | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1530+1688G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694229 | |||||||
chrX:154694391 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0002g0166 a0001c0001t0018g0087 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1530+1514_1530+152 others(16): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694391 | |||||||
chrX:154694391 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0002g0092 a0001c0001t0002g0100 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1530+1513_1530+152 others(17): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694391 | |||||||
chrX:154694425 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1530+1492G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694425 | |||||||
chrX:154694594 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1530+1323G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694594 | |||||||
chrX:154694596 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1530+1321A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694596 | |||||||
chrX:154694597 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1530+1320C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694597 | |||||||
chrX:154694979 | G | A | 10 | a0001c0001t0003g0031 a0001c0001t0003g0037 a0001c0001t0003g0044 others(7): Show |
10 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1530+938C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154694979 | |||||||
chrX:154695140 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1530+777A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154695140 | |||||||
chrX:154695296 | G | A | 12 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(9): Show |
12 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1530+621C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154695296 | |||||||
chrX:154695345 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1530+572G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154695345 | |||||||
chrX:154695684 | T | C | 7 | a0001c0001t0002g0007 a0001c0001t0002g0092 a0001c0001t0002g0100 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1530+233A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154695684 | |||||||
chrX:154695795 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0158 a0001c0001t0001g0160 |
3 | HG02293.hp2 NA18945.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1530+122G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154695795 | |||||||
chrX:154695907 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1530+10T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 8/9 | chrX | 154695907 | |||||||
chrX:154696029 | A | G | 5 | a0001c0001t0008g0002 a0001c0001t0008g0086 a0001c0001t0008g0090 others(2): Show |
8 | HG01884.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1428-10T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696029 | |||||||
chrX:154696298 | C | CA | 18 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0195 others(15): Show |
18 | HG00621.hp1 HG00673.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1428-280dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696298 | |||||||
chrX:154696298 | CA | C | 42 | a0001c0001t0001g0062 a0001c0001t0001g0094 a0001c0001t0001g0107 others(39): Show |
43 | HG00099.hp1 HG01069.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.1428-280delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696298 | |||||||
chrX:154696692 | T | C | 21 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(18): Show |
24 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1427+440A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696692 | |||||||
chrX:154696801 | G | A | 9 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0076 others(6): Show |
14 | HG00733.hp1 HG01074.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1427+331C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696801 | |||||||
chrX:154696957 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0158 a0001c0001t0001g0160 |
3 | HG02293.hp2 NA18945.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1427+175G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696957 | |||||||
chrX:154696980 | G | C | 1 | a0001c0001t0009g0208 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1427+152C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696980 | |||||||
chrX:154696994 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1427+138G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 7/9 | chrX | 154696994 | |||||||
chrX:154697462 | C | T | 3 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 |
3 | HG02055.hp1 HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1346-249G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/9 | chrX | 154697462 | |||||||
chrX:154697482 | A | T | 20 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(17): Show |
23 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1346-269T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/9 | chrX | 154697482 | |||||||
chrX:154697970 | C | A | 1 | a0001c0001t0001g0023 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1346-757G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/9 | chrX | 154697970 | |||||||
chrX:154697995 | T | C | 1 | a0001c0001t0018g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1346-782A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/9 | chrX | 154697995 | |||||||
chrX:154698153 | T | C | 37 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0043 others(34): Show |
38 | HG00621.hp1 HG01928.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.1346-940A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/9 | chrX | 154698153 | |||||||
chrX:154698511 | C | CT | 8 | a0001c0001t0002g0007 a0001c0001t0002g0092 a0001c0001t0002g0100 others(5): Show |
9 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1345+782dupA | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/9 | chrX | 154698511 | |||||||
chrX:154698552 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1345+742G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 6/9 | chrX | 154698552 | |||||||
chrX:154699756 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1126-243G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 5/9 | chrX | 154699756 | |||||||
chrX:154700119 | C | T | 1 | a0001c0001t0018g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1070-60G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154700119 | |||||||
chrX:154700259 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1070-200A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154700259 | |||||||
chrX:154700521 | C | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0166 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1070-462G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154700521 | |||||||
chrX:154700522 | A | G | 7 | a0001c0001t0002g0007 a0001c0001t0002g0092 a0001c0001t0002g0100 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-463T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154700522 | |||||||
chrX:154700898 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1070-839C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154700898 | |||||||
chrX:154700934 | G | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(234): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1070-875C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154700934 | |||||||
chrX:154702117 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1070-2058G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154702117 | |||||||
chrX:154702406 | C | G | 1 | a0004c0005t0002g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1070-2347G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154702406 | |||||||
chrX:154702434 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1070-2375G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154702434 | |||||||
chrX:154702704 | A | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00621.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1070-2645T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154702704 | |||||||
chrX:154702923 | A | G | 1 | a0001c0001t0007g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1070-2864T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154702923 | |||||||
chrX:154703397 | A | G | 3 | a0001c0001t0010g0084 a0001c0002t0002g0193 a0001c0002t0010g0051 |
3 | HG03130.hp1 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1070-3338T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154703397 | |||||||
chrX:154703459 | A | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(124): Show |
135 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1070-3400T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154703459 | |||||||
chrX:154703736 | G | A | 10 | a0001c0001t0003g0031 a0001c0001t0003g0037 a0001c0001t0003g0044 others(7): Show |
10 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1070-3677C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154703736 | |||||||
chrX:154703935 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1070-3876G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154703935 | |||||||
chrX:154704276 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1070-4217C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154704276 | |||||||
chrX:154704350 | G | T | 5 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | HG02040.hp1 HG02083.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070-4291C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154704350 | |||||||
chrX:154704599 | G | T | 1 | a0001c0001t0003g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1070-4540C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154704599 | |||||||
chrX:154704870 | A | C | 56 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0032 others(53): Show |
62 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1070-4811T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154704870 | |||||||
chrX:154704982 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1070-4923A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154704982 | |||||||
chrX:154704996 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1070-4937T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154704996 | |||||||
chrX:154705485 | C | G | 10 | a0001c0001t0002g0178 a0001c0001t0006g0035 a0001c0001t0006g0194 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1070-5426G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154705485 | |||||||
chrX:154705748 | G | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0092 a0001c0001t0002g0100 others(3): Show |
7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-5689C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154705748 | |||||||
chrX:154705823 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0002g0166 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1070-5764T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154705823 | |||||||
chrX:154706059 | A | C | 1 | a0001c0001t0002g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1070-6000T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706059 | |||||||
chrX:154706137 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0104 |
2 | NA18943.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1070-6078G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706137 | |||||||
chrX:154706412 | T | C | 1 | a0001c0006t0019g0233 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1069+5817A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706412 | |||||||
chrX:154706415 | C | CA | 32 | a0001c0001t0002g0239 a0001c0001t0003g0031 a0001c0001t0003g0037 others(29): Show |
35 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1069+5813dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706415 | |||||||
chrX:154706415 | CA | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1069+5813delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706415 | |||||||
chrX:154706631 | G | T | 1 | a0001c0002t0010g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1069+5598C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706631 | |||||||
chrX:154706747 | T | TA | 21 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(18): Show |
24 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1069+5481dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706747 | |||||||
chrX:154706921 | G | GA | 110 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(107): Show |
115 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1069+5307dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706921 | |||||||
chrX:154706921 | GA | G | 24 | a0001c0001t0002g0079 a0001c0001t0003g0045 a0001c0001t0003g0177 others(21): Show |
27 | HG00642.hp1 HG01081.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1069+5307delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154706921 | |||||||
chrX:154707040 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0148 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1069+5189A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154707040 | |||||||
chrX:154707058 | T | C | 1 | a0001c0001t0005g0204 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1069+5171A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154707058 | |||||||
chrX:154707123 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1069+5106G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154707123 | |||||||
chrX:154707520 | T | C | 21 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(18): Show |
24 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1069+4709A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154707520 | |||||||
chrX:154707869 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1069+4360A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154707869 | |||||||
chrX:154708105 | A | T | 1 | a0001c0002t0010g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1069+4124T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708105 | |||||||
chrX:154708107 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1069+4122T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708107 | |||||||
chrX:154708193 | C | T | 1 | a0001c0001t0012g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1069+4036G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708193 | |||||||
chrX:154708244 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0215 a0001c0001t0002g0240 |
4 | HG03041.hp1 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069+3985G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708244 | |||||||
chrX:154708279 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0057 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1069+3950T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708279 | |||||||
chrX:154708361 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1069+3868A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708361 | |||||||
chrX:154708615 | C | T | 11 | a0001c0001t0003g0031 a0001c0001t0003g0037 a0001c0001t0003g0044 others(8): Show |
11 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1069+3614G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708615 | |||||||
chrX:154708656 | C | G | 1 | a0001c0001t0003g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1069+3573G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708656 | |||||||
chrX:154708980 | C | A | 1 | a0001c0001t0018g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1069+3249G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154708980 | |||||||
chrX:154709134 | C | T | 96 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0144 others(93): Show |
103 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1069+3095G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709134 | |||||||
chrX:154709141 | T | C | 96 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0144 others(93): Show |
103 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1069+3088A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709141 | |||||||
chrX:154709144 | A | T | 96 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0144 others(93): Show |
103 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1069+3085T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709144 | |||||||
chrX:154709145 | C | CTT | 96 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0144 others(93): Show |
103 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1069+3083_1069+308 others(6): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709145 | |||||||
chrX:154709145 | C | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(95): Show |
103 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.1069+3084G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709145 | |||||||
chrX:154709171 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+3058T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709171 | |||||||
chrX:154709172 | A | T | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+3057T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709172 | |||||||
chrX:154709176 | A | G | 123 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0144 others(120): Show |
130 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.1069+3053T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709176 | |||||||
chrX:154709178 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(91): Show |
99 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1069+3051C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709178 | |||||||
chrX:154709180 | T | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+3049A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709180 | |||||||
chrX:154709180 | T | C | 1 | a0001c0001t0005g0206 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1069+3049A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709180 | |||||||
chrX:154709181 | TCCTTCCT others(847): Show |
T | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2194_1069+304 others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709181 | |||||||
chrX:154709194 | T | C | 1 | a0001c0001t0005g0119 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1069+3035A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709194 | |||||||
chrX:154709254 | T | C | 1 | a0001c0001t0003g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1069+2975A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709254 | |||||||
chrX:154709255 | G | C | 1 | a0001c0001t0003g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1069+2974C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709255 | |||||||
chrX:154709256 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1069+2973C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709256 | |||||||
chrX:154709282 | C | A | 1 | a0001c0001t0009g0208 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1069+2947G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709282 | |||||||
chrX:154709322 | GT | G | 194 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(191): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1069+2906delA | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709322 | |||||||
chrX:154709359 | C | T | 17 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(14): Show |
20 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1069+2870G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709359 | |||||||
chrX:154709390 | G | C | 1 | a0001c0002t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1069+2839C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709390 | |||||||
chrX:154709406 | T | C | 4 | a0004c0005t0002g0049 a0004c0005t0002g0050 a0004c0005t0002g0053 others(1): Show |
4 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069+2823A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709406 | |||||||
chrX:154709470 | G | A | 1 | a0001c0001t0005g0204 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1069+2759C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709470 | |||||||
chrX:154709509 | A | G | 7 | a0001c0001t0002g0007 a0001c0001t0002g0092 a0001c0001t0002g0100 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1069+2720T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709509 | |||||||
chrX:154709894 | C | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0158 a0001c0001t0001g0160 |
3 | HG02293.hp2 NA18945.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1069+2335G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709894 | |||||||
chrX:154709953 | G | C | 67 | a0001c0001t0002g0017 a0001c0001t0002g0067 a0001c0001t0002g0068 others(64): Show |
72 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1069+2276C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154709953 | |||||||
chrX:154710039 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2190A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710039 | |||||||
chrX:154710040 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2189C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710040 | |||||||
chrX:154710044 | A | T | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2185T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710044 | |||||||
chrX:154710045 | T | G | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2184A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710045 | |||||||
chrX:154710050 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2179A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710050 | |||||||
chrX:154710056 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2173C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710056 | |||||||
chrX:154710057 | T | C | 204 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(201): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1069+2172A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710057 | |||||||
chrX:154710058 | A | T | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2171T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710058 | |||||||
chrX:154710059 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2170T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710059 | |||||||
chrX:154710060 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2169A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710060 | |||||||
chrX:154710069 | C | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2160G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710069 | |||||||
chrX:154710070 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2159T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710070 | |||||||
chrX:154710072 | AATGCATA others(24): Show |
A | 10 | a0001c0001t0002g0017 a0001c0001t0002g0067 a0001c0001t0002g0068 others(7): Show |
10 | HG01358.hp1 HG02602.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+2126_1069+215 others(35): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710072 | |||||||
chrX:154710075 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2154C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710075 | |||||||
chrX:154710078 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2151A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710078 | |||||||
chrX:154710081 | G | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2148C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710081 | |||||||
chrX:154710085 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2144T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710085 | |||||||
chrX:154710086 | T | G | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2143A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710086 | |||||||
chrX:154710088 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2141T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710088 | |||||||
chrX:154710090 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2139T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710090 | |||||||
chrX:154710091 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2138A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710091 | |||||||
chrX:154710095 | C | G | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2134G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710095 | |||||||
chrX:154710096 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2133T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710096 | |||||||
chrX:154710106 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2123C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710106 | |||||||
chrX:154710113 | C | G | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2116G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710113 | |||||||
chrX:154710118 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2111T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710118 | |||||||
chrX:154710120 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1069+2109T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710120 | |||||||
chrX:154710621 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1069+1608C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154710621 | |||||||
chrX:154711050 | T | A | 79 | a0001c0001t0001g0107 a0001c0001t0001g0195 a0001c0001t0001g0211 others(76): Show |
85 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1069+1179A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711050 | |||||||
chrX:154711096 | G | C | 1 | a0001c0001t0003g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1069+1133C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711096 | |||||||
chrX:154711187 | C | A | 3 | a0001c0001t0002g0092 a0001c0001t0002g0100 a0001c0001t0002g0166 |
3 | HG02258.hp1 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1069+1042G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711187 | |||||||
chrX:154711388 | T | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(155): Show |
168 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(165): Show |
intron_variant | MODIFIER | c.1069+841A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711388 | |||||||
chrX:154711475 | G | C | 2 | a0001c0002t0002g0193 a0001c0002t0010g0051 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1069+754C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711475 | |||||||
chrX:154711515 | T | C | 17 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(14): Show |
20 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1069+714A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711515 | |||||||
chrX:154711564 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1069+665T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711564 | |||||||
chrX:154711954 | G | C | 1 | a0004c0005t0002g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1069+275C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154711954 | |||||||
chrX:154712135 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1069+94G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 4/9 | chrX | 154712135 | |||||||
chrX:154712977 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.596+230T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 3/9 | chrX | 154712977 | |||||||
chrX:154713742 | C | CAT | 38 | a0001c0001t0001g0026 a0001c0001t0001g0060 a0001c0001t0001g0061 others(35): Show |
39 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.377-318_377-317dup others(2): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | C | CATAT | 48 | a0001c0001t0001g0025 a0001c0001t0001g0140 a0001c0001t0001g0141 others(45): Show |
50 | HG00609.hp1 HG01123.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.377-320_377-317dup others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | C | CATATAT | 56 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0040 others(53): Show |
64 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.377-322_377-317dup others(6): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | C | CATATATA others(1): Show |
17 | a0001c0001t0001g0041 a0001c0001t0001g0057 a0001c0001t0001g0058 others(14): Show |
17 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.377-324_377-317dup others(8): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | C | CATATATA others(3): Show |
5 | a0001c0001t0001g0054 a0001c0001t0001g0230 a0001c0001t0001g0232 others(2): Show |
5 | HG00639.hp2 HG01891.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-326_377-317dup others(10): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | C | CATATATA others(5): Show |
4 | a0001c0001t0002g0067 a0001c0001t0002g0071 a0001c0001t0003g0177 others(1): Show |
4 | HG03654.hp1 HG03942.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-328_377-317dup others(12): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0228 |
2 | HG02293.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.377-330_377-317dup others(14): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | C | CATATATA others(9): Show |
1 | a0001c0001t0005g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.377-332_377-317dup others(16): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CAT | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0001t0002g0028 others(13): Show |
17 | HG00140.hp1 HG00642.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.377-318_377-317del others(2): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATAT | C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0107 others(6): Show |
9 | HG01099.hp1 HG01109.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-320_377-317del others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATATAT | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0154 others(4): Show |
7 | HG02040.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-322_377-317del others(6): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATATATA others(3): Show |
C | 2 | a0001c0002t0002g0030 a0001c0002t0010g0052 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.377-326_377-317del others(10): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATATATA others(5): Show |
C | 3 | a0001c0001t0009g0097 a0001c0002t0002g0036 a0004c0005t0002g0091 |
3 | HG01934.hp1 HG02622.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.377-328_377-317del others(12): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATATATA others(7): Show |
C | 5 | a0001c0001t0002g0100 a0001c0002t0010g0051 a0004c0005t0002g0049 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-330_377-317del others(14): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATATATA others(11): Show |
C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0215 |
3 | HG03041.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.377-334_377-317del others(18): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATATATA others(13): Show |
C | 1 | a0001c0001t0015g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.377-336_377-317del others(20): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713742 | CATATATA others(17): Show |
C | 1 | a0002c0003t0001g0155 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.377-340_377-317del others(24): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713742 | |||||||
chrX:154713805 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.377-379A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154713805 | |||||||
chrX:154714220 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.377-794A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154714220 | |||||||
chrX:154714346 | G | A | 11 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(8): Show |
11 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.377-920C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154714346 | |||||||
chrX:154714369 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.377-943G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154714369 | |||||||
chrX:154715136 | A | G | 1 | a0001c0001t0005g0204 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.376+890T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715136 | |||||||
chrX:154715373 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.376+653C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715373 | |||||||
chrX:154715397 | TGTGTGTG others(1): Show |
T | 11 | a0001c0001t0002g0239 a0001c0002t0002g0030 a0001c0002t0002g0036 others(8): Show |
11 | HG01109.hp1 HG01891.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.376+621_376+628del others(8): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715397 | |||||||
chrX:154715419 | T | G | 1 | a0001c0002t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.376+607A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715419 | |||||||
chrX:154715420 | G | C | 1 | a0001c0002t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.376+606C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715420 | |||||||
chrX:154715421 | C | A | 1 | a0001c0002t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.376+605G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715421 | |||||||
chrX:154715423 | T | A | 1 | a0001c0002t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.376+603A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715423 | |||||||
chrX:154715428 | CAGAG | C | 10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG00735.hp1 HG01123.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+594_376+597del others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715428 | |||||||
chrX:154715458 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.376+568G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715458 | |||||||
chrX:154715955 | C | T | 11 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(8): Show |
11 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.376+71G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 2/9 | chrX | 154715955 | |||||||
chrX:154716497 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.73-168A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154716497 | |||||||
chrX:154716683 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.73-354G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154716683 | |||||||
chrX:154717211 | C | A | 2 | a0001c0002t0004g0048 a0001c0002t0010g0052 |
2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.73-882G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154717211 | |||||||
chrX:154717327 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(137): Show |
150 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.73-998C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154717327 | |||||||
chrX:154717722 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.73-1393A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154717722 | |||||||
chrX:154717795 | A | G | 1 | a0001c0001t0003g0108 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.73-1466T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154717795 | |||||||
chrX:154718498 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-2169G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154718498 | |||||||
chrX:154718725 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.73-2396A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154718725 | |||||||
chrX:154718907 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-2578A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154718907 | |||||||
chrX:154719065 | G | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0134 a0001c0001t0002g0135 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-2736C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154719065 | |||||||
chrX:154719660 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-3331C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154719660 | |||||||
chrX:154719706 | G | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(138): Show |
151 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.73-3377C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154719706 | |||||||
chrX:154719885 | C | T | 141 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(138): Show |
151 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.73-3556G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154719885 | |||||||
chrX:154720138 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0215 |
3 | HG03041.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.73-3809T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720138 | |||||||
chrX:154720388 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0015g0019 others(1): Show |
4 | HG01109.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-4059T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720388 | |||||||
chrX:154720403 | T | G | 4 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0015g0019 others(1): Show |
4 | HG01109.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-4074A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720403 | |||||||
chrX:154720412 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(137): Show |
150 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.73-4083C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720412 | |||||||
chrX:154720498 | C | T | 10 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(7): Show |
10 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-4169G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720498 | |||||||
chrX:154720605 | C | T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0016 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.73-4276G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720605 | |||||||
chrX:154720626 | C | CA | 37 | a0001c0001t0001g0107 a0001c0001t0001g0121 a0001c0001t0001g0157 others(34): Show |
38 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.73-4298dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720626 | |||||||
chrX:154720626 | CA | C | 12 | a0001c0001t0001g0133 a0001c0001t0001g0228 a0001c0001t0007g0130 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.73-4298delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720626 | |||||||
chrX:154720755 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0002g0240 others(2): Show |
5 | HG01109.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-4426G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720755 | |||||||
chrX:154720901 | C | T | 1 | a0001c0001t0012g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.73-4572G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720901 | |||||||
chrX:154720942 | C | T | 140 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(137): Show |
150 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.73-4613G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720942 | |||||||
chrX:154720981 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-4652G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154720981 | |||||||
chrX:154721074 | T | C | 1 | a0001c0001t0007g0131 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.73-4745A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154721074 | |||||||
chrX:154721339 | C | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(153): Show |
166 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(163): Show |
intron_variant | MODIFIER | c.73-5010G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154721339 | |||||||
chrX:154721518 | G | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(153): Show |
166 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(163): Show |
intron_variant | MODIFIER | c.73-5189C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154721518 | |||||||
chrX:154721561 | T | A | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-5232A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154721561 | |||||||
chrX:154721832 | C | A | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-5503G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154721832 | |||||||
chrX:154721965 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.73-5636T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154721965 | |||||||
chrX:154722267 | A | T | 17 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0004g0218 others(14): Show |
20 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.73-5938T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154722267 | |||||||
chrX:154722360 | G | T | 152 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(149): Show |
162 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.73-6031C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154722360 | |||||||
chrX:154722791 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.73-6462C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154722791 | |||||||
chrX:154723040 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.73-6711C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154723040 | |||||||
chrX:154723256 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-6927T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154723256 | |||||||
chrX:154723266 | G | A | 5 | a0001c0001t0007g0003 a0001c0001t0007g0130 a0001c0001t0007g0131 others(2): Show |
8 | HG00673.hp1 NA18944.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-6937C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154723266 | |||||||
chrX:154723872 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(152): Show |
165 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(162): Show |
intron_variant | MODIFIER | c.73-7543G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154723872 | |||||||
chrX:154723960 | T | G | 1 | a0004c0005t0002g0091 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.73-7631A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154723960 | |||||||
chrX:154724055 | C | T | 10 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(7): Show |
10 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-7726G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724055 | |||||||
chrX:154724144 | C | T | 4 | a0001c0001t0007g0003 a0001c0001t0007g0130 a0001c0001t0007g0131 others(1): Show |
7 | NA18944.hp1 NA18953.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-7815G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724144 | |||||||
chrX:154724145 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-7816C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724145 | |||||||
chrX:154724218 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.73-7889C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724218 | |||||||
chrX:154724342 | T | TTAAA | 21 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0098 others(18): Show |
22 | HG00280.hp1 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-8017_73-8014dup others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724342 | |||||||
chrX:154724342 | TTAAA | T | 8 | a0001c0001t0001g0107 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
8 | HG01099.hp1 HG02004.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-8017_73-8014del others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724342 | |||||||
chrX:154724342 | TTAAATAA others(1): Show |
T | 6 | a0001c0001t0003g0038 a0001c0002t0002g0030 a0001c0002t0002g0036 others(3): Show |
6 | HG01934.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-8021_73-8014del others(8): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724342 | |||||||
chrX:154724342 | TTAAATAA others(5): Show |
T | 1 | a0001c0001t0016g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.73-8025_73-8014del others(12): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724342 | |||||||
chrX:154724850 | C | T | 4 | a0001c0001t0008g0002 a0001c0001t0008g0086 a0001c0001t0008g0090 others(1): Show |
7 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-8521G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154724850 | |||||||
chrX:154725067 | G | A | 10 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(7): Show |
10 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-8738C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154725067 | |||||||
chrX:154725348 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.73-9019G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154725348 | |||||||
chrX:154725526 | T | A | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-9197A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154725526 | |||||||
chrX:154726792 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-10463A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154726792 | |||||||
chrX:154727014 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0015g0019 others(1): Show |
4 | HG01109.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-10685T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154727014 | |||||||
chrX:154727170 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-10841G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154727170 | |||||||
chrX:154727380 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-11051G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154727380 | |||||||
chrX:154727455 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-11126T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154727455 | |||||||
chrX:154727497 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.73-11168A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154727497 | |||||||
chrX:154727829 | C | T | 1 | a0001c0001t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.73-11500G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154727829 | |||||||
chrX:154727881 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-11552G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154727881 | |||||||
chrX:154728124 | G | C | 1 | a0001c0001t0016g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.73-11795C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154728124 | |||||||
chrX:154728183 | C | T | 1 | a0001c0001t0004g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-11854G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154728183 | |||||||
chrX:154728362 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.73-12033C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154728362 | |||||||
chrX:154728460 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.73-12131C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154728460 | |||||||
chrX:154728651 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-12322G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154728651 | |||||||
chrX:154728843 | A | C | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-12514T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154728843 | |||||||
chrX:154728928 | G | A | 10 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(7): Show |
10 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-12599C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154728928 | |||||||
chrX:154729415 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-13086G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154729415 | |||||||
chrX:154729753 | G | A | 11 | a0001c0001t0002g0046 a0001c0002t0002g0030 a0001c0002t0002g0036 others(8): Show |
11 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-13424C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154729753 | |||||||
chrX:154730047 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.73-13718C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154730047 | |||||||
chrX:154730339 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.73-14010A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154730339 | |||||||
chrX:154730377 | C | T | 9 | a0001c0001t0002g0046 a0001c0002t0002g0030 a0001c0002t0002g0036 others(6): Show |
9 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-14048G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154730377 | |||||||
chrX:154730573 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-14244C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154730573 | |||||||
chrX:154730586 | G | C | 4 | a0001c0001t0001g0043 a0001c0001t0003g0031 a0001c0001t0003g0037 others(1): Show |
4 | NA18948.hp1 NA18963.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-14257C>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154730586 | |||||||
chrX:154732442 | T | G | 4 | a0001c0001t0008g0002 a0001c0001t0008g0086 a0001c0001t0008g0090 others(1): Show |
7 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-16113A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154732442 | |||||||
chrX:154732600 | A | C | 1 | a0001c0001t0003g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.73-16271T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154732600 | |||||||
chrX:154732733 | A | G | 5 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0002g0240 others(2): Show |
5 | HG01109.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-16404T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154732733 | |||||||
chrX:154733231 | A | C | 10 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(7): Show |
10 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-16902T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154733231 | |||||||
chrX:154733714 | G | A | 2 | a0001c0001t0002g0073 a0001c0001t0002g0074 |
2 | HG01358.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.72+17240C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154733714 | |||||||
chrX:154733785 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.72+17169A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154733785 | |||||||
chrX:154733802 | T | C | 1 | a0001c0001t0003g0044 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.72+17152A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154733802 | |||||||
chrX:154734373 | C | A | 10 | a0001c0001t0001g0195 a0001c0001t0006g0035 a0001c0001t0006g0194 others(7): Show |
10 | HG01243.hp1 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+16581G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154734373 | |||||||
chrX:154735018 | CTAAT | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(152): Show |
165 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(162): Show |
intron_variant | MODIFIER | c.72+15932_72+15935d others(6): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735018 | |||||||
chrX:154735167 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.72+15787C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735167 | |||||||
chrX:154735312 | C | G | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+15642G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735312 | |||||||
chrX:154735321 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+15633T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735321 | |||||||
chrX:154735339 | A | G | 1 | a0002c0003t0001g0127 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.72+15615T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735339 | |||||||
chrX:154735481 | T | C | 146 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(143): Show |
156 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.72+15473A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735481 | |||||||
chrX:154735502 | C | G | 10 | a0001c0002t0002g0030 a0001c0002t0002g0036 a0001c0002t0002g0066 others(7): Show |
10 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+15452G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735502 | |||||||
chrX:154735670 | C | G | 1 | a0001c0001t0014g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.72+15284G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735670 | |||||||
chrX:154735781 | C | T | 6 | a0001c0002t0004g0048 a0001c0002t0010g0051 a0001c0002t0010g0052 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+15173G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735781 | |||||||
chrX:154735792 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.72+15162C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154735792 | |||||||
chrX:154736028 | T | C | 5 | a0001c0001t0003g0034 a0001c0001t0003g0085 a0001c0001t0003g0174 others(2): Show |
5 | HG01261.hp1 NA18941.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+14926A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736028 | |||||||
chrX:154736132 | C | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0166 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.72+14822G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736132 | |||||||
chrX:154736185 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+14769C>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736185 | |||||||
chrX:154736219 | A | C | 11 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0002g0240 others(8): Show |
11 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+14735T>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736219 | |||||||
chrX:154736575 | C | A | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+14379G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736575 | |||||||
chrX:154736634 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+14320G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736634 | |||||||
chrX:154736680 | G | A | 1 | a0001c0001t0006g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72+14274C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736680 | |||||||
chrX:154736917 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0165 |
2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.72+14037T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736917 | |||||||
chrX:154736941 | C | T | 15 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0002g0240 others(12): Show |
15 | HG01109.hp1 HG01891.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.72+14013G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154736941 | |||||||
chrX:154737056 | T | A | 1 | a0001c0001t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.72+13898A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154737056 | |||||||
chrX:154737144 | A | T | 1 | a0001c0001t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.72+13810T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154737144 | |||||||
chrX:154737483 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+13471C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154737483 | |||||||
chrX:154737514 | A | T | 1 | a0001c0001t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.72+13440T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154737514 | |||||||
chrX:154737564 | A | T | 1 | a0001c0001t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.72+13390T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154737564 | |||||||
chrX:154737575 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.72+13379C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154737575 | |||||||
chrX:154737666 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.72+13288G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154737666 | |||||||
chrX:154738262 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.72+12692C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154738262 | |||||||
chrX:154738509 | A | T | 3 | a0001c0001t0002g0234 a0001c0001t0002g0236 a0001c0001t0003g0235 |
3 | HG02257.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.72+12445T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154738509 | |||||||
chrX:154738765 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.72+12189G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154738765 | |||||||
chrX:154739030 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+11924G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154739030 | |||||||
chrX:154739127 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+11827C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154739127 | |||||||
chrX:154739696 | GACAGAGG others(19): Show |
G | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+11232_72+11257d others(28): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154739696 | |||||||
chrX:154739725 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0215 |
3 | HG03041.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.72+11229T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154739725 | |||||||
chrX:154740081 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+10873G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154740081 | |||||||
chrX:154740315 | T | C | 1 | a0001c0001t0006g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.72+10639A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154740315 | |||||||
chrX:154740585 | C | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(154): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.72+10369G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154740585 | |||||||
chrX:154740956 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.72+9998C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154740956 | |||||||
chrX:154741601 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0005g0203 |
2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.72+9353C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154741601 | |||||||
chrX:154741607 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.72+9347G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154741607 | |||||||
chrX:154741675 | C | CA | 7 | a0001c0001t0001g0165 a0001c0001t0002g0100 a0001c0001t0002g0103 others(4): Show |
7 | HG02258.hp1 HG02602.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+9278dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154741675 | |||||||
chrX:154741675 | CA | C | 9 | a0001c0001t0001g0025 a0001c0001t0002g0012 a0001c0001t0002g0013 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+9278delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154741675 | |||||||
chrX:154741696 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.72+9258T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154741696 | |||||||
chrX:154742055 | C | A | 1 | a0001c0001t0003g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.72+8899G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742055 | |||||||
chrX:154742059 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.72+8895G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742059 | |||||||
chrX:154742219 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.72+8735T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742219 | |||||||
chrX:154742491 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.72+8463A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742491 | |||||||
chrX:154742494 | T | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | NA18990.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.72+8460A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742494 | |||||||
chrX:154742707 | C | G | 1 | a0001c0001t0002g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.72+8247G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742707 | |||||||
chrX:154742985 | C | CAT | 38 | a0001c0001t0001g0117 a0001c0001t0002g0075 a0001c0001t0002g0104 others(35): Show |
41 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.72+7967_72+7968dup others(2): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742985 | |||||||
chrX:154742985 | C | CATAT | 37 | a0001c0001t0001g0055 a0001c0001t0001g0107 a0001c0001t0001g0172 others(34): Show |
38 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.72+7965_72+7968dup others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742985 | |||||||
chrX:154742985 | C | CATATAT | 5 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0006g0194 others(2): Show |
5 | HG03669.hp2 HG03704.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+7963_72+7968dup others(6): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742985 | |||||||
chrX:154742985 | CAT | C | 4 | a0001c0001t0001g0217 a0001c0001t0002g0016 a0001c0001t0005g0168 others(1): Show |
4 | HG01884.hp2 HG03130.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+7967_72+7968del others(2): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742985 | |||||||
chrX:154742985 | CATATAT | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(11): Show |
14 | HG01081.hp1 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.72+7963_72+7968del others(6): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154742985 | |||||||
chrX:154743549 | T | C | 1 | a0001c0002t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.72+7405A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154743549 | |||||||
chrX:154743881 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.72+7073T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154743881 | |||||||
chrX:154744018 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.72+6936T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744018 | |||||||
chrX:154744019 | T | A | 1 | a0001c0001t0002g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.72+6935A>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744019 | |||||||
chrX:154744082 | C | T | 27 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(24): Show |
32 | HG00099.hp1 HG00733.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.72+6872G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744082 | |||||||
chrX:154744108 | G | A | 1 | a0001c0001t0014g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.72+6846C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744108 | |||||||
chrX:154744212 | C | CA | 90 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(87): Show |
96 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.72+6741dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744212 | |||||||
chrX:154744212 | C | CAA | 29 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0180 others(26): Show |
29 | HG00673.hp1 HG01261.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.72+6740_72+6741dup others(2): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744212 | |||||||
chrX:154744212 | CA | C | 15 | a0001c0001t0001g0020 a0001c0001t0002g0017 a0001c0001t0002g0239 others(12): Show |
15 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+6741delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744212 | |||||||
chrX:154744212 | CAAAAAAA others(4): Show |
C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
15 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+6731_72+6741del others(11): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744212 | |||||||
chrX:154744536 | A | G | 6 | a0001c0002t0004g0048 a0001c0002t0010g0051 a0001c0002t0010g0052 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+6418T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744536 | |||||||
chrX:154744884 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(12): Show |
15 | HG01081.hp1 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.72+6070G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744884 | |||||||
chrX:154744958 | A | G | 1 | a0001c0001t0004g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.72+5996T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154744958 | |||||||
chrX:154745047 | T | C | 1 | a0001c0001t0006g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.72+5907A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154745047 | |||||||
chrX:154745129 | C | T | 1 | a0001c0002t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.72+5825G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154745129 | |||||||
chrX:154745742 | C | A | 3 | a0001c0001t0001g0020 a0001c0001t0015g0019 a0001c0001t0017g0018 |
3 | HG02922.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72+5212G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154745742 | |||||||
chrX:154745777 | C | A | 1 | a0001c0001t0005g0214 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.72+5177G>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154745777 | |||||||
chrX:154745944 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72+5010G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154745944 | |||||||
chrX:154746007 | G | A | 27 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0001t0001g0211 others(24): Show |
27 | HG00735.hp2 HG01243.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.72+4947C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746007 | |||||||
chrX:154746052 | C | CA | 5 | a0001c0001t0001g0217 a0001c0001t0002g0009 a0001c0001t0002g0215 others(2): Show |
6 | HG03041.hp1 HG03139.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+4901dupT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746052 | |||||||
chrX:154746052 | CA | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0003g0031 others(3): Show |
6 | HG00140.hp1 HG02735.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+4901delT | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746052 | |||||||
chrX:154746069 | AAAAG | A | 10 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(7): Show |
10 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+4881_72+4884del others(4): Show |
GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746069 | |||||||
chrX:154746108 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.72+4846T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746108 | |||||||
chrX:154746177 | C | G | 1 | a0001c0002t0002g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.72+4777G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746177 | |||||||
chrX:154746408 | T | G | 237 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(234): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.72+4546A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746408 | |||||||
chrX:154746816 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | NA18612.hp1 NA19012.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+4138G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154746816 | |||||||
chrX:154747044 | C | T | 1 | a0001c0001t0006g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72+3910G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747044 | |||||||
chrX:154747156 | C | T | 1 | a0001c0001t0013g0021 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.72+3798G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747156 | |||||||
chrX:154747223 | G | A | 6 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG00621.hp1 HG02027.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+3731C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747223 | |||||||
chrX:154747289 | G | A | 3 | a0001c0001t0002g0234 a0001c0001t0002g0236 a0001c0001t0003g0235 |
3 | HG02257.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.72+3665C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747289 | |||||||
chrX:154747612 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.72+3342C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747612 | |||||||
chrX:154747789 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.72+3165A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747789 | |||||||
chrX:154747826 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+3128C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747826 | |||||||
chrX:154747926 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.72+3028C>T | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154747926 | |||||||
chrX:154748180 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72+2774T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154748180 | |||||||
chrX:154748410 | C | G | 5 | a0001c0001t0001g0020 a0001c0001t0002g0239 a0001c0001t0002g0240 others(2): Show |
5 | HG01109.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+2544G>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154748410 | |||||||
chrX:154748727 | T | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.72+2227A>G | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154748727 | |||||||
chrX:154749314 | A | T | 1 | a0001c0001t0005g0011 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.72+1640T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154749314 | |||||||
chrX:154749438 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.72+1516G>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154749438 | |||||||
chrX:154749468 | A | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+1486T>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154749468 | |||||||
chrX:154749845 | A | T | 1 | a0001c0001t0005g0011 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.72+1109T>A | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154749845 | |||||||
chrX:154749961 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.72+993A>C | GAB3 | ENSG00000160219.12 | transcript | ENST00000424127.3 | protein_coding | 1/9 | chrX | 154749961 |